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JCPSP-Journal of the College of Physicians and Surgeons Pakistan. 2004; 14 (10): 628-30
en Inglés | IMEMR | ID: emr-66352

RESUMEN

Tuberous sclerosis is a rare genetic disease of autosomal dominant inheritance, associated with hamartomata formation in several organs and various skin findings. A case of young male is presented here with multiple fibromas on right side of his face, peri-ungual fibromas in right index and middle fingers and right second toe, a small shagreen plaque over right lower back and multiple, ill-defined hypopigmented patches over his right side of the trunk and right buttocks. Fundoscopic examination revealed retinal phacomas on right side. CT-scan brain showed right-sided paraventricular calcification


Asunto(s)
Humanos , Masculino , Esclerosis Tuberosa/terapia , Hamartoma/diagnóstico , Fibroma/diagnóstico , Piel/patología
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